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deck_5488790 Flashcards

1
Q

Most breast cancers arise where?

A

In the terminal duct lobular unit (TDLU) consisting of the terminal ducts, the lobules, and the surrounding stroma

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2
Q

What are the most common palpable lesions of the breast?

A

cysts, fibroadenomas, and invasive carcinomas

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3
Q

These are the histopathologic findings in a series of women seeking evaluation of breast ‘lumps’

A
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4
Q

Approximately 50% of carcinomas are located in what part of the breast?

A

the upper outer quadrantNOTE:Only 10% of breast masses in women younger than age 40 are malignant as compared with 60% of masses in women older than age 50 (this number drops off around 80 yo)the majority of cancers that have the capacity to metastasize will have done so by the time they reach a size that can be palpated—generally around 2 to 3 cm.

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5
Q

What are the major symptoms of breast disease (in order)?

A

lumpiness or palpable masspainnipply discharge

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6
Q

What are the common common causes for nipple pain?

A

fibrocystic changes that are cyclic with the menstrual period ordue to obstruction or inflammation (especially in breastfeeding women)NOTE: Only about 10% of breast cancers are painful

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7
Q

Bloody nipple discharge suggest what?

A

large duct papiloma

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8
Q

Why would it make sense to group fibrocystic breast changes into non-proliferative vs. proliferative changes?

A

Non-proliferative changes have a very small chance of transforming into cancer

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9
Q

What are fibrocystic changes?

A

These are the most common breast abnormality in pre-menopausal women and are most likely to be a consequence of the cyclic breast changes that occur normally during the menstrual cycle and result in either some form of fibrosis or cyst formation

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10
Q

Does estrogen therapy increase the risk of fibrocystic change? What about oral contraceptives?

A

No to either, and oral contraceptives may actually decrease the risk

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11
Q

Describe the morphology of non-proliferative fibrocytic changes in the breast

A

A single, large cyst may form within one breast, but changes are usually multifocal that appear as ill-defined, diffusely increased densities and nodules on mammography.Unopened cysts are brown to blue in color (blue dome cysts) and are filled with fluid and secretions that may calcify to produce microcalcifications on mammaograms

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12
Q

What is this showing?

A

There is a very pink epithelium characteristic of a nonproliferative cyst. Frequently, the lining cells are large and polygonal with eosinophilic cytoplasm, a process called apocrine metaplasia which is virtually always benign

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13
Q

What is this showing?

A

Apocrine metaplasia, which is almost always benign

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14
Q

Normal ducts and lobules of the breast are lined by what?

A

two layers of cells- a layer of luminal cells overlying a second layer of myoepithelial cellsNOTE: In order to diagnose an invasive carcinoma, these layers must be destroyed.

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15
Q

What is a common sign of proliferative change?

A

epithelial hyperplasia, or the presence of more than two layers of cells lining to ducts and lobules of the breast (increas

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16
Q

What are the types of epithelial hyperplasia?

A

usual duct hyperplasia (below- note that slitlike fenestrations in the duct lumen) and atypical duct hyperplasia

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17
Q

What is this showing?

A

Atypical ductal hyperplasia-is recognized by its histologic resemblance to ductal carcinoma in situ (DCIS). It consists of a relatively monomorphic proliferation of regularly spaced cells (with no overlap), sometimes with cribriform spaces.Most surgeons will remove cells with atypical ductal hyperplasia

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18
Q

What is this?

A

Atypical lobular hyperplasia-consists of cells identical to those of lobular carcinoma in situ, but the cells do not fill or distend more than 50% of the acini within a lobule.Surgeons typically do not surgically excise these cells

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19
Q

What is sclerosing adenosis (aka too many glands)?

A

A type of fibrocystic change that is less common than cysts and hyperplasia but is significant because it mimics carcinoma closely.The involved terminal duct lobular unit is enlarged, and the acini are compressed and distorted by dense stroma.Calcifications are present within some of the lumens.Unlike carcinomas, the acini are arranged in a swirling pattern, and the outer border is well circumscribed.The acini at the edge of a focus of sclerosing adenosis appear round and smoothly contoured. They possess a two-layered epithelium composed of both luminal and myoepithelial cells, and a basement membrane encloses each acinus.

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20
Q

What types of fibrocystic changes have minimal or no increased risk of breast carcinoma?

A

fibrosis, cystic changes, apocrine metaplasia, and mild hyperplasia

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21
Q

What types of fibrocystic changes have slightlyincreased (1.5-2x) risk of breast carcinoma?

A

moderate to florid hyperplasia (without atypia), ductal papillomatosis, sclerosing adenosis

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22
Q

What types of fibrocystic changes have significantly increased risk of breast carcinoma?

A

atypical hyperplasia, whether ductal or lobular, DCIS, and LCIS

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23
Q

How do inflammatory processes of the breast typically present?

A

They are uncommon and are usually associated with pain and tenderness in the affected areas

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24
Q

What are some causes of inflammation in the breast?

A

Acute mastitisFat encrosisMammary duct ectasiaLymphocytic mastitisGranulomatous mastitis

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25
Q

What is the most common cause of acute mastitis?

A

It typically develops when bacteria, usually Staph aureus, gain access to breast tissue through the ducts, typically during breastfeedingand typically presents as single or mutiple abscesses. Usually found in the lateral breast

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26
Q

What causes fat necrosis in the breast?

A

It is an uncommon lesion that produces a mass, typically as the result of trauma that presents as a central focus of necrotic fat surrounded by neutrophils that later becomes enclosed by firous tissue and is eventually replaced by scar tissue or a cyst.Calcifications may also develop in either the scar or cyst wall

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27
Q

What causes mammary duct ectasia?

A

a nonbacterial chronic inflammation associated with nipple obstruction most commonly. Ductal dilation and eventual rupture leads to reactive changes in the surrounding tissue that may present as a poorly defined periareolar mass with nipple retraction (mimics some cancer).

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28
Q

What are some known associations with lymphocytic mastitis?

A

Diabetes and possibly autoimmune

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29
Q

What are the common tumors of the breast?

A

¤Fibroadenoma (FA)¤Phyllodes Tumor¤Intraductal papilloma¤Carcinoma¤Gynecomastia

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30
Q

What are fibroadenomas?

A

The most common neoplasm of the female breast (especially common in women in their 30s), it is a biphasic tumor composed of fibroblastic stroma and epithelium-lined glands (but only the stromal cells are clonal are truly neoplastic)

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31
Q

Describe the gross appearance of fibroadenomas. How are they diagnosed?

A

They are usually discrete, firm, and mobile (feels rubbery and compressable) and on cut-section take on a uniform tan-white color, with softer yellow-pink specks representing the glandular areas.Diagnosis is made by needle-core biopsy or excision

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32
Q

What causes fibroadenomas?

A

They are thought to be controlled by estrogen and characteristically can enlarge late in the menstrual cycle and during pregnancy and may regress and calcify after menopause

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33
Q

How do fibroadenomas appear histologically?

A

They are characterized by a loss fibroblastic stroma containing ductlike, epithelium-lined spaces

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34
Q

What are phyllodes tumors?

A

These are also biphasic, being composed of neoplastic cells and epithelium-lined glands. However, they can be distinguished from fibroadenomas because they are more cellular and form epithelium-lined leaflife projectionsThese arise de novo and are usually benign

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35
Q

Phyllodes tumors can be malignant. What are some indicators of a malignant prognosis?

A

increased stromal cellularity, rapid size increase, 10+ mitotic figures,and infiltrative margins.NOTE: Even malignant tumors tend to remain localized (85%)Be suspicious about a ‘fibroadenoma’ if it is large (> 35mm) and from an older woman (> 35 yrs)The surgeon may alert you to a history of recent growth

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36
Q 
                 Benign Borderline MalignantPushing boundary        Yes    Usually  Not usuallyStromal/epithelial balance Even    Even    UnevenStromal cellularity         High    High      HighVariab.of stromal cellularity:Yes    Yes      Yes ++Stromal mitoses /10 hpf     < 5     5 - 10     >10
A

Phyloddes prognosis

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37
Q

What are Intraductal papillomas?

A

Benign neoplastic papillary growth most often seen in premenopausal women, and commonly found within the principal lactiferous ducts or sinuses.

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38
Q

How do intraductal papillomas tend to present?

A

-serous or blood nipple discharge-the presence of a small subareolar tumor a few millimeters in diameter-nipple retraction in rare cases

39
Q

Describe what you see

A

Intraductal papillomaA central fibrovascular core extends from the wall of a duct.The papillae arborize within the lumen and are lined by myoepithelial and luminal cells.

40
Q

How common is breast cancer in women?

A

It is the most common cancer in women and the 2nd highest killer of women behind lung cancer (40K/yr). The lifetime risk of developing breast cancer is 1 in 8Prevalence: In 2012, there were an estimated 2,975,314 women living with breast cancer in the United States.

41
Q

What are the risk factors for developing breast cancer?

A

-age (especially after menopause and peaking at age 80)-higher in the US and northern europe-race (higher in white women, but hispanics and AA are more likely to develop it at a younger age and to have more aggressive tumors)-prolonged exposure to exogenous estrogen postmenopausally (i.e. for the use of osteoporosis)-ionizing radiation to the chest (but only in younger women- under 30)-obesity, alcohol, and high fat diet

42
Q

Why would obesity lead to increased risk of breast cancer?

A

Because of increased estrogen produced by adipose tissue

43
Q

What are some things that do NOT raise the risk of breast cancer?

A

-oral contraceptives-low doses of radiation associated with mammogram screening

44
Q

What is this?

A

breast carcinoma

45
Q

Although the exact pathogenesis of breast cancer remain incompletely understood, there are three main parts of its development, namely:

A

-genetic changes-hormonal influences-environmental variables

46
Q

How common is HER2/NEU proto-oncogene overexpression in breast cancer development?

A

It is amplified in up to 30% of invasive breast cancers. This gene is a member of the epidermal growth factor receptor family and its overexpression is associated with a poor prognosis

47
Q

Other mutations common in breast cancer?

A

-Amplification of RAS ans MYC-mutations of RB and TP53-BRCA 1/2

48
Q

Gene expression profiling can separate breast cancer into what four molecular subtypes?

A

1) Luminal A (ER +, HER2/NEU -)2) Luminal B (ER +; HER2/NEU overexpressing)3) HER2/NEU positive (HER/NEU overexpressing; ER -)4) Basal like (ER-; HER2/NEU -)

49
Q

What percentage of breast cancer is linked to inherited mutations?

A

10%. These are more likely to be bilateral, assoicated with other cancers, have a Fam Hx, to develop before menopause, and have BRCA mutations

50
Q

What are BRCA 1/2?

A

Tumor suppressor genes (Thus, both alleles must be inactivated to cause cancer)

51
Q

Describe BRCA 1

A

This tumor suppressor gene is located at 17q21 and is:oADoBRCA1 mutations are present in 10% of women with (a) no family history, (b) breast cancer onset by age 40 years, and (c) high grade, triple negative tumorsobreast cancer usually developsby ages 40-59

52
Q

What are the most effective predictors of BRCA1 mutation?

A

age of onset under50 years, and triple negative status

53
Q

What are some other genetic diseases assoicated with breast cancer?

A

Li-Faumeni SyndromeCowden Syndrome (PTEN mutation)Ataxia-telangiectsia gene carriers

54
Q

How would a women with a known BRCA1 mutation (but not actually breast cancer yet)be treated?

A

Carriers are subject to close foolw-up or prophylactic mastectomy-Tamoxifen may prevent bilateral breast cancers in ER negative tumors-Increased risk of recurrence after breast conserving surgery-BRCA1 status does not appear to affect death rates, but is associated with resistance certain chemotherapy agents

55
Q

What histo manifestations may indicate an increased likelihood that BRCA1 mutations may be present?

A

There may be:-Usually high grade (basal-like phenotype)-abundant intra- and peritumoral lymphocytes-Greater incidence of medullary tumors-High incidence of DCIS

56
Q

BRCA2

A

oUsually get breast cancer by age 50oPatients also have higher risk of cancers of ovary (39-63%), bone, pharynx, prostate, pancreas; also other organsSlightly more frequent in black (2.6%) versus white (2.1%) American patients

57
Q

Where is BRCA2 located?

A

chromosome 13q12-13

58
Q

What is the micro-description of BRCA2 mutations in the breast?

A

The micro appearance isnt as useful as in BRCA1oUsually invasive ductal carcinoma, no special typeoHigh grade features and pushing tumor marginoHigh incidence of DCIS

59
Q

What hormonal influences may lead to an increased risk of breast cancer?

A

Estrogen excess, or hormonal imbalance has a clear role. Many of the risk factors (long duration of reproductive life, nulliparity, and late age of birth of the first child) are related to exposure of estrogen unopposed by progesterone. Functional ovarian tumors may also increase estrogen production

60
Q

How does estrogen promote tumor development?

A

It stimulates production of growth factors, such as transforming growth factor-a, PDGF, and FGF which promote tumor development

61
Q

Breast cancers are classified according to whether they have or not penetrated the basement membrane. What are some non-invasive breast cancers?

A
  1. Ductal carcinoma in situ2. Lobular carcinoma in situThese tumors still have both levels of membrane
62
Q

What are someinvasive breast cancers?

A
  1. Invasive ductal carcinoma2. Invasive lobular carcinoma3. Medullary carcinoma4. Colloid carcinoma (mucinous carcinoma)5. Tubular carcinoma6. Other
63
Q

Both DCIS and LCIS arise from where?

A

cells in the terminal duct lobular unit

64
Q

What is this?

A

This is a variant of ductal carcinoma in situ (cribiform). Of the many potential appearances of DCIS, incouding papillary, solid, comedo, and clinging types, all can present with necrosis, especially comedo.Another frequent assoication with DCIS is the presence of calcifications

65
Q

What is the prognosis of DCIS?

A

97% long term survival after simple mastectomy.

66
Q

What are the treatment options of DCIS?

A

Current treatment options include lumpectomy, radiation and antiestrogenic agents such as tamoxifen and aromatase

67
Q

What is this?

A

High grade comedo type DCIS- marked by a central, prominent necrosis and mitotic figures. There is abut a 30% chance of local invasion so most pts. opt to surgically remove. These often show calcifications that can be picked up by mammography

68
Q

What causes Paget disease of the nipple?

A

extension of DCIS up the lactiferous ducts into nipple skin

69
Q

What is this?

A

LCIS marked by uniform, monomorphic cells, loss of e-cadherin, and intracellular mucin filled vacuoles(rarely associated with calcifications so mammogram might not pick up)

70
Q

How is LCIS treated?

A

either chemotherapy or close follow-up

71
Q

How do LCIS progress?

A

1/3 of women with LCIS will develop invasive carcinoma. Unlike DCIS, subsequent invasive carcinomas may arise in either breast

72
Q

What are invasive ductal carcinomas?

A

A term for all carcinomas that do not fit other categories (represent 70-80% of invasive breast tumors)NOTE: These arisefrom terminal duct lobular units (as dolobular carcinomas), not ductal epithelium, so nomenclature is not actually accurate

73
Q

IDC is usually associated with _____

A

DCIS, and rarely LCIS

74
Q

What is the key to diagonsis of a IDC?

A

NO myoepithelial cell layer

75
Q

What is this?

A

IDC- again, there is a lack of of myoepithelial cells surrounding the tumor cells

76
Q

Describe invasive lobular carcinomas

A

Typically arise from and mimic LCIS. The tumor cells individually invaded the strome and often align in ‘single-file’ strands or chains and again, are commonly associated with loss of function mutationsof CDH1 , the gene that encodes E-cadherin

77
Q

Mutations in CDH1 is also assoicated with what?

A

Males and females with heterozygous germline mutations in CDH1 also have a greatly increased risk of gastric signet ring cell carcinoma.

78
Q

Describe what is being seen in these lobular duct carcinomas

A

Top: the loss of E-caderins results in lining of cellsBottom: targetoid vacuoles can be seen and mucin can be seen pushing the nuclei to the side

79
Q

How do invasive lobular carcinomas spread?

A

they spread to CSF, serosal surfaces, the GI tract, and bone marrow

80
Q

Describe medullary carcinomas of the breast

A

These are very rare characterized by a high level of lymphplasmacytic infiltrate (DCIS is usually absen tor minimal)

81
Q

Medullary carcinomas ocur

A
82
Q

T or F. Medullary carcinomas tend to be triple negative

A

T. They lack estrogen andprogesterone receptors AND do not overexpress HER2/NEU

83
Q

What are some histological characteristics of medullary carcinomas of the breast?

A

•Indistinct cell borders (syncytial growth)•Large pleomorphic tumor cells containing large nuclei, prominent nucleoli, numerous mitotic figures•Prominent lymphoplasmacytic infiltrate at periphery•Pushing borders / well circumscribed and not as invasive (which is probably why these pts. Have a good prognosis- easy to remove)

84
Q

What is this?

A

A colloid/mucinous carcinoma, in which histologically tumor cells can be seen floating in large amounts of mucinThese tumors are slow-growing, found in women over 70 yo, and have a great 10 yr survival rate. On gross exam, these tumors feel gelantous and soft.

85
Q

Describe tubular carcinomas

A

These are rare tumors that have a favorable prognosis and arecomposed of:•distinct, well-differentiated angular tubular structures (90%+ according to WHO) with•open lumina,• lined by a single layer of epithelial cells

86
Q

T or F. Tubular carcinomas express hormone receptors but do not show HER2/NEU overexpression

A

T.

87
Q

What is this?

A

Micropapillary variant of breast carcinoma- these are very aggressive (95% have lymph node metastases at presentation;70% recur, 50% die of disease) and have a poor prognosis

88
Q

What is this showing?

A

Paget Disease of the nipple- This presents as a slow growing, itchy rash rash over the nipple (confused with allergic dermatitis) and characterized by epidermal infiltration by malignant glandular cells and commonly an underlying carcinoma

89
Q

What is inflammatory carcinoma?

A

The clinical presentation of an enlarged, swollen, breast usually without a palpable mass and an underlyingductal carcinoma that is poorly differentiatedwith invasion of dermal lymphatics. This can mimic infection.The prognosis is very bad

90
Q

What is this?

A

Peau d-orange appearance- this is commonly due to invasive cancers adhereing to pectoral muscle or deep fascia in the breast and resulting dimpling, as well as blocked lymphatics

91
Q

What is the main use of mammography?

A

It can help identify breast masses before they are palpable, at which time 50% are already metastasizing

92
Q

Why is mammogram screeening better in older women?

A

breast becomes more fatty and easier to visualize

93
Q

Gynecomastia

A

Histologically men have no lobules, so it is marked by increased ducts and prominent stroma – maybe edematous with increased cellularity, late phase may have fibrosisPhysiologic can occur in puberty and old age

94
Q

What are some of the main causes of gynecomastia?

A

Causes include cirrhosis (liver cannot metabolize estrogen), Klinefelter syndrome, anabolic steroids, and drugs

step pathology (80 decks)

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